34087
Diethofencarb
PESTANAL®, analytical standard
Synonym(s):
Isopropyl N-(3,4-diethoxyphenyl)carbamate
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About This Item
Empirical Formula (Hill Notation):
C14H21NO4
CAS Number:
Molecular Weight:
267.32
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
Recommended Products
grade
analytical standard
Quality Level
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
application(s)
agriculture
environmental
format
neat
SMILES string
CCOc1ccc(NC(=O)OC(C)C)cc1OCC
InChI
1S/C14H21NO4/c1-5-17-12-8-7-11(9-13(12)18-6-2)15-14(16)19-10(3)4/h7-10H,5-6H2,1-4H3,(H,15,16)
InChI key
LNJNFVJKDJYTEU-UHFFFAOYSA-N
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General description
Diethofencarb is a systemic, phenyl-carbamate fungicide, used for the control of gray mold on fruits and vegetables. Its mode of action involves the inhibition of phospholipids and fatty acid biosynthesis in pathogens.
Application
Diethofencarb may be used as an analytical reference standard for the determination of the analyte in peel and pulp of apples using dispersive liquid-liquid microextraction, followed by high-performance liquid chromatography with diode-array detection (HPLC-DAD).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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D W Hollomon et al.
Antimicrobial agents and chemotherapy, 42(9), 2171-2173 (1998-09-16)
Benzimidazoles are important antitubulin agents used in veterinary medicine and plant disease control. Resistance is a practical problem correlated with single amino acid changes in beta-tubulin and is often linked to greater sensitivity to phenylcarbamates. This negative cross-resistance creates opportunities
M Fujimura et al.
Current genetics, 21(4-5), 399-404 (1992-04-01)
Two MBC-resistant mutants of Neurospora crassa, F914 and F939, were sensitive to diethofencarb at a concentration of 0.1 micrograms/ml, while the wild-type strain and other MBC-resistant mutants showed resistance to diethofencarb at a concentration of 100 micrograms/ml. Genetic analysis suggested
K Saito et al.
Xenobiotica; the fate of foreign compounds in biological systems, 21(5), 575-582 (1991-05-01)
1. Age-related changes in metabolism of diethofencarb (DFC) (isopropyl-1,4-diethoxycarbanilate) and hepatic drug-metabolizing enzyme activities were studied in male Sprague-Dawley rats aged 2, 8, 16 and 21 months. 2. Following a single oral dose of 14C-DFC (500 mg/kg), the major route
Rika Kodaka et al.
Journal of agricultural and food chemistry, 51(26), 7730-7737 (2003-12-11)
The unique nitration of the carbamate fungicide diethofencarb (Powmyl, isopropyl 3,4-diethoxycarbanilate) was examined in 14 Japanese soils and three types of clays under the aerobic conditions using the (14)C-labeled compound. Nitration at the 6-position of the 3,4-diethoxyphenyl ring was a
Jing Cheng et al.
International journal of environmental analytical chemistry, 90(11), 845-855 (2010-09-24)
Dispersive liquid-liquid microextraction (DLLME) has been developed for the extraction and preconcentration of diethofencarb (DF) and pyrimethanil (PM) in environmental water. In the method, a suitable mixture of extraction solvent (50 μL carbon tetrachloride) and dispersive solvent (0.75 mL acetonitrile)
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